28181366 33987182 31648317 32990483 30600763 31069978 34304778 31124578 32208489 28637620 28179279 28659335 31097629 32089214 30083851 - Search Results

Year	Number of Results
2017	4
2018	1
2019	5
2020	4
2021	3
2022	0

1

Molecular phenotype and bleeding risks of an inherited platelet disorder in a family with a RUNX1 frameshift mutation.

Badin MS, Iyer JK, Chong M, Graf L, Rivard GE, Waye JS, Paterson AD, Pare G, Hayward CPM. Badin MS, et al. Haemophilia. 2017 May;23(3):e204-e213. doi: 10.1111/hae.13169. Epub 2017 Feb 8. Haemophilia. 2017. PMID: 28181366

2

Zebrafish Cancer Predisposition Models.

Kobar K, Collett K, Prykhozhij SV, Berman JN. Kobar K, et al. Front Cell Dev Biol. 2021 Apr 27;9:660069. doi: 10.3389/fcell.2021.660069. eCollection 2021. Front Cell Dev Biol. 2021. PMID: 33987182 Free PMC article. Review.

3

ClinGen Myeloid Malignancy Variant Curation Expert Panel recommendations for germline RUNX1 variants.

Luo X, Feurstein S, Mohan S, Porter CC, Jackson SA, Keel S, Chicka M, Brown AL, Kesserwan C, Agarwal A, Luo M, Li Z, Ross JE, Baliakas P, Pineda-Alvarez D, DiNardo CD, Bertuch AA, Mehta N, Vulliamy T, Wang Y, Nichols KE, Malcovati L, Walsh MF, Rawlings LH, McWeeney SK, Soulier J, Raimbault A, Routbort MJ, Zhang L, Ryan G, Speck NA, Plon SE, Wu D, Godley LA. Luo X, et al. Blood Adv. 2019 Oct 22;3(20):2962-2979. doi: 10.1182/bloodadvances.2019000644. Blood Adv. 2019. PMID: 31648317 Free PMC article.

4

Distinctive phenotypes in two children with novel germline RUNX1 mutations - one with myeloid malignancy and increased fetal hemoglobin.

Bagla S, Regling KA, Wakeling EN, Gadgeel M, Buck S, Zaidi AU, Flore LA, Chicka M, Schiffer CA, Chitlur MB, Ravindranath Y. Bagla S, et al. Pediatr Hematol Oncol. 2021 Feb;38(1):65-79. doi: 10.1080/08880018.2020.1814463. Epub 2020 Sep 29. Pediatr Hematol Oncol. 2021. PMID: 32990483

5

Bone Marrow Morphology Associated With Germline RUNX1 Mutations in Patients With Familial Platelet Disorder With Associated Myeloid Malignancy.

Chisholm KM, Denton C, Keel S, Geddis AE, Xu M, Appel BE, Cantor AB, Fleming MD, Shimamura A. Chisholm KM, et al. Pediatr Dev Pathol. 2019 Jul-Aug;22(4):315-328. doi: 10.1177/1093526618822108. Epub 2019 Jan 2. Pediatr Dev Pathol. 2019. PMID: 30600763

6

Inherited thrombocytopenia and platelet disorders with germline predisposition to myeloid neoplasia.

Galera P, Dulau-Florea A, Calvo KR. Galera P, et al. Int J Lab Hematol. 2019 May;41 Suppl 1:131-141. doi: 10.1111/ijlh.12999. Int J Lab Hematol. 2019. PMID: 31069978 Review.

7

Molecular Genetics of Pediatric Acute Myeloid Leukemia.

Krock B, Oberley MJ. Krock B, et al. Clin Lab Med. 2021 Sep;41(3):497-515. doi: 10.1016/j.cll.2021.03.014. Epub 2021 Jul 1. Clin Lab Med. 2021. PMID: 34304778 Review.

8

Longitudinal sequencing of RUNX1 familial platelet disorder: new insights into genetic mechanisms of transformation to myeloid malignancies.

Duarte BKL, Yamaguti-Hayakawa GG, Medina SS, Siqueira LH, Snetsinger B, Costa FF, Rauh MJ, Ozelo MC. Duarte BKL, et al. Br J Haematol. 2019 Sep;186(5):724-734. doi: 10.1111/bjh.15990. Epub 2019 May 24. Br J Haematol. 2019. PMID: 31124578

9

RUNX1-mutated families show phenotype heterogeneity and a somatic mutation profile unique to germline predisposed AML.

Brown AL, Arts P, Carmichael CL, Babic M, Dobbins J, Chong CE, Schreiber AW, Feng J, Phillips K, Wang PPS, Ha T, Homan CC, King-Smith SL, Rawlings L, Vakulin C, Dubowsky A, Burdett J, Moore S, McKavanagh G, Henry D, Wells A, Mercorella B, Nicola M, Suttle J, Wilkins E, Li XC, Michaud J, Brautigan P, Cannon P, Altree M, Jaensch L, Fine M, Butcher C, D'Andrea RJ, Lewis ID, Hiwase DK, Papaemmanuil E, Horwitz MS, Natsoulis G, Rienhoff HY, Patton N, Mapp S, Susman R, Morgan S, Cooney J, Currie M, Popat U, Bochtler T, Izraeli S, Bradstock K, Godley LA, Krämer A, Fröhling S, Wei AH, Forsyth C, Mar Fan H, Poplawski NK, Hahn CN, Scott HS. Brown AL, et al. Blood Adv. 2020 Mar 24;4(6):1131-1144. doi: 10.1182/bloodadvances.2019000901. Blood Adv. 2020. PMID: 32208489 Free PMC article.

10

RUNX1 deficiency (familial platelet disorder with predisposition to myeloid leukemia, FPDMM).

Schlegelberger B, Heller PG. Schlegelberger B, et al. Semin Hematol. 2017 Apr;54(2):75-80. doi: 10.1053/j.seminhematol.2017.04.006. Epub 2017 Apr 13. Semin Hematol. 2017. PMID: 28637620 Review.

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